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临床试验/CTRI/2020/05/025059
CTRI/2020/05/025059招募中未知

Tuberculosis (TB) Aftermath

ational Institutes Of Health NIH USA0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Those who are registered at one of the study TB Units (TUs) in Pune district as treatment completed or cured (regardless of type of TB or duration of treatment).
  • 2. Confirmed treatment completion or cure status by the referring medical officer of the study TU.
  • 3. Date of treatment completion within 60 days of date of enrolment.
  • 4. Ability and willingness of participant or legal guardian/representative to provide informed consent to participate in Arm 1 House Hold Active Case Finding (HHACF) or Arm 2 Active case finding through telephone(TACF)
  • (NOTE: Illiterate participants or participants with cognitive disabilities may be enrolled based on local regulatory policies, with the appropriate provisions for informed consent.)
  • 5. All household contacts of TB cases who are able and willing to provide informed consent to participate are eligible. HH contacts who are <18 years old are eligible for enrolment if a legal guardian/representative provides informed consent.

排除标准

  • 1. Completed anti-TB treatment at a private sector clinic or TU outside of the study (final visit not registered at one of the study TB units)
  • 2. Actively on anti-TB treatment

研究者

发起方
ational Institutes Of Health NIH USA

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